FDA UDI In Commercial Distribution 🇺🇸 United States

LUMINDEX

DI: 04719873921775 · Model: LUMINDEX 3 · DENTMATE TECHNOLOGY CO., LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LUMINDEX
Primary DI
04719873921775
Version / Model
LUMINDEX 3
Company Name
DENTMATE TECHNOLOGY CO., LTD.
Labeler DUNS
656134660
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-17
Public Version
2
Public Version Date
2023-08-03
Public Version Status
Update
Public Device Record Key
3951aed2-bdb4-40c0-b1ad-891eba6ce94f

Device Description

LUMINDEX 3 (Dentmate)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HJN Transilluminator, Battery-Powered

GMDN Terms

Code Name
36761 Visible-light skin transilluminator

Identifiers

Type ID
Primary 04719873921775